78686-80-3 Usage
Uses
Used in Chemical and Pharmaceutical Research:
6-Bromo-5-chloro-nicotinic acid methyl ester is employed as a building block or intermediate in the synthesis of various organic compounds. Its unique structure and functional groups make it a valuable component in the development of new chemical entities.
Used in Agrochemical Production:
6-BroMo-5-chloro-nicotinic acid Methyl ester is utilized in the production of agrochemicals, which are chemicals used in agricultural processes to enhance crop yield and protect plants from pests and diseases. Its chemical properties contribute to the effectiveness of these products.
Used in Pharmaceutical Production:
6-Bromo-5-chloro-nicotinic acid methyl ester is also used in the manufacturing of pharmaceuticals, where it may serve as a key intermediate in the synthesis of drugs with potential therapeutic applications.
Used in Antimicrobial Applications:
6-Bromo-5-chloro-nicotinic acid methyl ester has been studied for its antimicrobial properties, which can be harnessed to develop new antimicrobial agents to combat resistant bacteria and other pathogens.
Used in Anti-inflammatory Applications:
Research has also explored the anti-inflammatory potential of 6-BroMo-5-chloro-nicotinic acid Methyl ester, suggesting its use in the development of anti-inflammatory drugs to treat various inflammatory conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 78686-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,8 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78686-80:
(7*7)+(6*8)+(5*6)+(4*8)+(3*6)+(2*8)+(1*0)=193
193 % 10 = 3
So 78686-80-3 is a valid CAS Registry Number.
78686-80-3Relevant academic research and scientific papers
Some Methyl 2,5- and 5,6-Dihalonicotinates
Setliff, Frank L.,Hule, W. Reeves
, p. 332 - 333 (2007/10/02)
The preparation of the methyl esters of eight dihalonicotinic acids is described.The esters were synthesized either by the methanolysis of their respective acid chlorides or by treatment of the appropriate acid with diazomethane in ether.Experimental and spectral data for the methyl dihalonicotinates are presented.
